WATERBRIGHT RADIATING
- Product NDC
- 54111-129
- 11-digit product format
- 541110129
- Labeler code
- 54111
- Product ID
- 54111-129_aec0734b-12b1-440a-a5d7-b8bbbda48428
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bentley Laboratories, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-06-01
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 2 g/50mL; g/50mL; g/50mL; g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54111-129-50 | WATERBRIGHT RADIATING | 50 mL in 1 TUBE | CREAM | 50 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54111-129 | WATERBRIGHT RADIATING (AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) CREAM [BENTLEY LABORATORIES, LLC] | 3 | Legacy NDC, 1 package rows | 20181220_85b4d3e4-240a-40cb-97f6-b293d1c9405f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 54111-129-50 | 54111012950 | 50 mL in 1 TUBE | 50 ml | Historical |